Cleared Traditional

K921496 - SKIN SAVER(TM) TUBING HOLDER, MODEL 1921 MODIFIED
(FDA 510(k) Clearance)

Aug 1992
Decision
158d
Days
Class 1
Risk

K921496 is an FDA 510(k) clearance for the SKIN SAVER(TM) TUBING HOLDER, MODEL 1921 MODIFIED. This device is classified as a Cannula, Nasal, Oxygen (Class I - General Controls, product code CAT).

Submitted by Alpine Specialties, Inc. (Loveland, US). The FDA issued a Cleared decision on August 14, 1992, 158 days after receiving the submission on March 9, 1992.

This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5340.

Submission Details

510(k) Number K921496 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 09, 1992
Decision Date August 14, 1992
Days to Decision 158 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Statement

Device Classification

Product Code CAT — Cannula, Nasal, Oxygen
Device Class Class I - General Controls
CFR Regulation 21 CFR 868.5340

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